Canonical Allele Identifier: CA423755187

Gene: ACTA1

Linked Data

• dbSNP Id: rs1571893092
• gnomAD v4: 1-229432127-G-A
• MyVariant Identifiers: chr1:g.229567874G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.229432127G>A , CM000663.2:g.229432127G>A	GRCh38
NC_000001.10:g.229567874G>A , CM000663.1:g.229567874G>A	GRCh37
NC_000001.9:g.227634497G>A	NCBI36
NG_006672.1:g.6970C>T , LRG_429:g.6970C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366683.4:c.675C>T	ENSP00000355644.4:p.Phe225=
ENST00000684723.1:c.540C>T	ENSP00000508084.1:p.Phe180=
ENST00000366683.3:c.480-265C>T	ENSP00000355644.3:n.480-265C>T
ENST00000366684.7:c.675C>T MANE Select	ENSP00000355645.3:p.Phe225=
NM_001100.3:c.675C>T , LRG_429t1:c.675C>T	NP_001091.1:p.Phe225=
NM_001100.4:c.675C>T MANE Select	NP_001091.1:p.Phe225=